ISO/IEEE 11073-10207:2019

ISO/IEEE
INTERNATIONAL
11073-10207
STANDARD
First edition
2019-03
Health informatics — Personal health
device communication —
Part 10207:
Domain information and service
model for service-oriented point-of-
care medical device communication
Informatique de santé — Communication entre dispositifs de santé
personnels —
Partie 10207: Informations de domaine et modèle de services pour la
communication orientée services entre dispositifs médicaux sur le site
des soins
Reference number
ISO/IEEE 11073-10207:2019(E)
©
IEEE 2018

---------------------- Page: 1 ----------------------
ISO/IEEE 11073-10207:2019(E)

COPYRIGHT PROTECTED DOCUMENT
© IEEE 2018
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from IEEE at the address below.
Institute of Electrical and Electronics Engineers, Inc
3 Park Avenue, New York
NY 10016-5997, USA
Email: stds.ipr@ieee.org
Website: www.ieee.org
Published in Switzerland
ii © IEEE 2018 – All rights reserved

---------------------- Page: 2 ----------------------
ISO/IEEE 11073-10207:2019(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national
standards bodies (ISO member bodies). The work of preparing International Standards is normally
carried out through ISO technical committees. Each member body interested in a subject for which a
technical committee has been established has the right to be represented on that committee.
International organizations, governmental and non-governmental, in liaison with ISO, also take part
in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all
matters of electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for
the different types of ISO documents should be noted (see www.iso.org/directives).
IEEE Standards documents are developed within the IEEE Societies and the Standards Coordinating
Committees of the IEEE Standards Association (IEEE-SA) Standards Board. The IEEE develops its
standards through a consensus development process, approved by the American National Standards
Institute, which brings together volunteers representing varied viewpoints and interests to achieve
the final product. Volunteers are not necessarily members of the Institute and serve without
compensation. While the IEEE administers the process and establishes rules to promote fairness in
the consensus development process, the IEEE does not independently evaluate, test, or verify the
accuracy of any of the information contained in its standards.
Attention is drawn to the possibility that some of the elements of this document may be the subject
of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details
of any patent rights identified during the development of the document will be in the Introduction
and/or on the ISO list of patent declarations received (see www.iso.org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT), see
www.iso.org/iso/foreword.html.
ISO/IEEE 11073-10207 was prepared by the IEEE 11073 Standards Committee of the IEEE
Engineering in Medicine and Biology Society (as IEEE Std 11073-10207-2017) and drafted in
accordance with its editorial rules. It was adopted, under the “fast-track procedure” defined in the
Partner Standards Development Organization cooperation agreement between ISO and IEEE, by
Technical Committee ISO/TC 215, Health informatics.
A list of all parts in the ISO 11073 series can be found on the ISO website.
Any feedback or questions on this document should be directed to the user’s national standards
body. A complete listing of these bodies can be found at www.iso.org/members.html.
© IEEE 2018 – All rights reserved
iii

---------------------- Page: 3 ----------------------
ISO/IEEE 11073-10207:2019(E)
Abstract: Within the context of the ISO/IEEE 11073™ family of standards for point-of-care
medical device communication, a Participant Model derived from the ISO/IEEE11073-10201
Domain Information Model is provided in this standard. The Participant Model specifies the
structure of medical information objects. This standard also define
...